Retinitis pigmentosa (RP) is a heterogeneous group of hereditary diseases characterized by
progressive degeneration of retinal photoreceptors leading to progressive visual decline. It …

Hereditary retinal diseases are now the leading cause of blindness certification in the
working age population (age 16–64 years) in England and Wales, of which retinitis …

Retinitis pigmentosa (RP) comprises a group of inherited retinal dystrophies characterized
by the degeneration of rod photoreceptors, followed by the degeneration of cone …

Background: Intravitreal injection (IVI) with administration of various pharmacological agents
is a mainstay of treatment in ophthalmology for endopthalmitis, viral retinitis, age-related …

Diabetic macular edema (DME), pseudophakic cystoid macular edema (CME), age‐related
macular degeneration (AMD), retinal vascular occlusion (RVO), and uveitis are ocular …

Aims: To determine the prevalence of cystoid macular oedema (CMO) in retinitis pigmentosa
(RP) patients of various genetic subtypes using optical coherence tomography (OCT) …

Background: Based on experimental studies and clinical observations by Robert Machemer,
Gholam Peyman and others, the vitreous cavity has increasingly been used as a reservoir of …

Retinitis pigmentosa (RP) is a diverse group of hereditary degenerations characterized by
progressive dysfunction of predominantly rod followed by cone photoreceptors. Typical RP …

There are various treatments for cystoid macular edema (CME) secondary to retinitis
pigmentosa; however, the evidence for these treatments has not been previously …

Intravitreal triamcinolone acetonide (IVTA) has increasingly been applied as treatment for
various intraocular neovascular and oedematous diseases. Comparing the various diseases …